B2.2: Organelles And Compartmentalization Flashcards

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1
Q

What are organelles?

A

Discrete structures within a cell that are adapted to preform a specific function

Can be solid structures or combination of dissolved solutes
(Plasma membrane is considered a organelle)

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2
Q

What does no/single/double membrane mean?
What are some examples of each?

A

No membrane: not enclosed by a phospholipid layer-> solid structure in cyto/nucleoplasm
- ribosomes
- centrioles
- nucleolus

Single membrane: enclosed by a single phospholipid bilayer
- Vesicles+vacuoles
- RER/SER
- golgi
- lysosome

Double membrane: enclosed by 2 phospholipid bilayers
- nucleus
- mitochondria
- chloroplast

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3
Q

What structures in a cell do not meet the requirements of an organelle?

A

Cell wall:
Outside of cell membrane (extracellular)
Not in cell -> not organelle

Cytoplasm:
Cytosol -> liquid part of cytoplasm, 80% water and dissolved solutes
Many metabolic reactions happen in cytoplasm -> but is not specialized to preform a specific function -> not organelle

Cytoskeleton:
Composed of many filaments and tubules
Not discrete -> not organelle

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4
Q

Outline why post-transcriptional modification of RNA is not possible in prokaryotic cells

A

In eukaryotic:
mRNA must undergo modification before being translated ->
Parts are removed/altered before leaving the nucleus

In prokaryotic:
No nucleus -> no altering/modifications

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5
Q

Explain how eukaryotic cells evolved to have compartments

A

Through infolding and endosymbiosis -> become super efficient spaces where many activites can happen at once

Membrane is only permeable to small number of substances, barrier between aqueous solutions, a compartment with controlled conditions

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6
Q

What are the advantages of compartmentalization?

A

compartments are separate from environment of surrounding cytosol
Tailored to function of organelle

Enzyme and substrate can be localized -> higher concentration

Damaging substances separated

Optimal conditions maintained for certain processes (efficiency)

Large areas of membrane becomes dense with proteins for a specific process -> location and number of organelles can be altered depending on the requirements of the cell

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7
Q

What are the advantages of compartmentalization in the nucleus?

A

Allow for genes to be separated
- genes that need to be expressed in differentiated cells can be copied and released into the cytoplasm
- genes that don’t need to be expressed -> stay in nucleus/inactive

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8
Q

What are the advantages of compartmentalization in the lysosome?

A

High concentration of enzymes -> can digest/hydrolyse all types of biological polymers

All lysosomal enzymes -> acid hydrolyses -> active at low pH -> maintained in lysosome

Double protection:
compartment allows for protection of other organelles
Neutral pH of cytoplasm would prevent hydrolase from digesting everything

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9
Q

Explain phagocytosis/phagocytic vacuole

A

Phagocytosis:
Process by which a cell uses its plasma membrane to engulf a large particle giving rise to a phagocytic vacuole/phagosome
Type of endocytosis

Cell that does this -> phagocytes
Fuses with lysosome to breakdown pathogen

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10
Q

What are the advantages of the double membrane of the nucleus? (Envelope and pore) (what is pore)

A

(Look on notes (B2.2.6) for info on the nucleus)

The nuclear envelope:
Nucleus surrounded by 2 concentric membranes (inner (INM) and outer (ONM))
Both are phospholipid bilayers
ONM continuous with RER
Protect genetic material in the cell and separates it from substances/chemical reaction in the cytoplasm

Nuclear pores (complex):
Selective passageway where small polar molecules/ions/macromolecules can travel (x30 size of ribosome)
large pore as a result of double membrane
Very big because:
Protein needed for genome structure and function synthesized at ribosomes in cytoplasm -> nucleus
mRNA and tRNA formed at nucleus (transcription) -> exported to cytoplasm
(for translation)
Ribosomes in nucleolus -> into cytoplasm/ER

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11
Q

What are the advantages of the double membrane of the nucleus? (Cell division)

A

(Look on notes (B2.2.6) for info on the nucleus)

Nucleus disassembles and reformes each time (most) cells divide

Prophase -> chromosomes condense and nucleolus disappears -> nuclear membrane fragmented into vesicles -> nuclear pore complex disappears

Final steps of cell division -> vesicles formed by nuclear membrane surround the chromosomes -> vesicles around each chromosome fuse -> double membrane around chromosomes -> vesicles fuses with each other -> complete nucleus and pore complexes reassemble

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12
Q

What is the endomembrane system?

A

System of compartmentalized sacs within a eukaryotic cell that work together to modify processes and ship molecules within/out of the cell

All organelles composed of phospholipids
- phospholipids can move within bilayer:
-> membrane flexible
Which allows for:
Formation of vesicles
Materials to be taken in (endocytosis) or out (exocytosis)
Pinching in of the membrane during animal cell cytokinesis

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13
Q

Rough endoplasmic reticulum and ribosome structure (as a part of the endomembrane system)

A

RER:
Series of connected and flattened membranous sacs with bound ribosomes
Ribosomes synthesize polypeptides and release to the inside of RER
RER -> elsewhere in cell by vesicle -> usually Golgi apparatus

Ribosomes structure:
Made of dozens of proteins arranged on a scaffold of ribosomal RNA (rRNA)
rRNA facilitates the binding of mRNA and tRNA + catalyzes the formation of peptide bonds between amino acids
2 subunits
Once’s assembled -> bind to mRNA and synthesize protein

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14
Q

Ribosome structure (as a part of the endomembrane system)

A

Ribosome -> catalyze and synthesis of polypeptides during translation

Free: floating in cytoplasm and synthesizes polypeptides used in the cell (ex: lysosome)

Bound: attached to RER and synthesizes polypeptides that are secreted from cell or used in the cell membrane

Signal sequence -> dictate if free go to RER or not
Signal sequences occur during beginning of polypeptide -> signal recognition protein bind to polypeptide, pauses translation -> free ribosome bind to a receptor on ER, forms RER -> translation starts again, polypeptide chain moves inside the ER

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15
Q

Structure and function of Golgi apparatus

A

Structure:
Flattened membrane-enclosed sacs called cisternae

Polypeptides synthesized by bound ribosomes on RER -> vesicle -> Golgi
Vesicle fuse with Golgi at cis face (entry face towards the RER/nucleus, convex) -> receives protein/lipid filled vesicles
Polypeptides -> Golgi -> exit via vesicles budding from concave trans face (exit face, usually towards the plasma membrane)

Function:
Polypeptide modified into functional state
- add carbohydrates to make glycoprotein
- combine with other polypeptides to form quaternary structure of protein

After modification -> functional protein

Trans face of Golgi sorts, concentrates and packs protein into vesicles for transport to lysosomes, membrane, exterior, etc.

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16
Q

Formation, movement and fusion of vesicles

A

Membrane-bound sacs used for transport and storage

Formation:
Formed when the membrane bulges and pinches off (result of membrane flexibility/phospholipids being able to move within the bilayer)
-> Golgi, membrane (endocytosis), RER

Clathrin -> protein that creates a coat to help the phospholipids create a rounded shape while the vesicle is forming (very important!)
- coat formed -> receptor proteins on cell surface bind to target molecules -> target molecules are attached -> cytoskeleton protein help clathrin pit to deepen and seal off -> trap target molecule inside

Movement:
Vesicles move through the cell along cytoskeleton track (motor proteins)

Fusion:
Merging of vesicle with another organelle or with part of a cell membrane
Adds phospholipids to the target structure -> larger

17
Q

Function of vesicles (the different types of vesicles)

A

Transport vesicles:
Transport proteins and lipids from one place to another within the cell

Secretory vesicles:
Transports protein and lipids from inside the cell to the plasma membrane
- integral protein within the plasma membrane (pumps; channels, adhesion/receptor proteins)
- hormones, neurotransmitters

Endocytic vesicles:
Formed by invagination of plasma membrane around an extra cellular substance during endocytosis
Deliver cargo to other organelles for further sorting/digestion (phagocytosis)

Other types include:
Peroxisomes - contain enzymes that digest fatty acids
Lysosomes - contain digestive enzymes which digest cellular waste/harmful substances

18
Q

Explain cell fractionation

A

Progress in science follows development of techniques -> study of function of individual organelles possible because inventions like cell fractionation

Cell fractionation -> a process that involves a pure sample (contains only the specific organelle being studied) and breaking up a sample of tissues then centrifuging the mixture at different speeds

3 stages:
Homogenization -> cell sample broken up using
homogenizer (blender adjacent)

Filtration -> homogenate is filtered through a gauze

Ultracentrifugation -> filtrate is placed into a tube and tube placed in centrifuge (separates materials based on density)
- speed altered to separate different components of cell based molecular weight

Until this was discovered -> research limited